Abstract
Immune checkpoint inhibitors (ICIs) have transformed the treatment paradigm for several malignancies. While the use of single-agent or combined ICIs has achieved acceptable disease control rates in a variety of solid tumors, such approaches have yet to show substantial therapeutic efficacy in select difficult-to-treat cancer types. Recently, select chemotherapy regimens are emerging as extensive modifiers of the tumor microenvironment, leading to the reprogramming of local immune responses. Accordingly, data is now emerging to suggest that certain anti-neoplastic agents modulate various immune cell processes, most notably the cross-presentation of tumor antigens, leukocyte trafficking, and cytokine biosynthesis. As such, the combination of ICIs and cytotoxic chemotherapy are beginning to show promise in many cancers that have long been considered poorly responsive to ICI-based immunotherapy. Here, we discuss past and present attempts to advance chemo-immunotherapy in these difficult-to-treat cancer histologies, mechanisms through which select chemotherapies modify tumor immunogenicity, as well as important considerations when designing such approaches to maximize efficacy and improve therapeutic response rates.
Original language | English (US) |
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Article number | 108111 |
Journal | Pharmacology and Therapeutics |
Volume | 236 |
DOIs | |
State | Published - Aug 2022 |
Funding
This article is dedicated to the memory of our good friend Daniel J. Takala who recently passed away after a courageous battle with glioblastoma. This work was supported by NIH F30CA236031 and UIC Award for Graduate Research to D.R. Principe, by NIH R01CA07059 to M. Korc, and by NIH R01CA217907 , R21CA255291 , and the Veterans Affairs Merit Award I01BX002922 to H.G. Munshi.
Keywords
- Cancer
- Chemotherapy
- Immune checkpoint inhibitors
- Immunology
- Tumor microenvironment
ASJC Scopus subject areas
- Pharmacology (medical)
- Pharmacology